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Research 151–180 of 1000+
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- The clinical management of hirsutism
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Ocular Cosmetics in Modern Times
- Loose Anagen Hair Syndrome in Black‐Haired Indian Children
- Successful Hair Transplantation of Recalcitrant Alopecia Areata of the Scalp
- Hair loss in children.
- Alopecia associated with strontium ranelate use in a 62-year-old woman
- Hair Lightening of Three Hemodialysis Patients Under Heptaminol
- Short Anagen Syndrome in an Indian Woman with its Impact on Quality-of-Life
- Alopecia in a 19-Month-Old Boy
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Minimal Incision Lateral Temporal Brow lift: An Evaluation Study
- Loose anagen hair syndrome presenting as patchy hypotrichosis – clinico-trichoscopic correlation
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Acitretin for the Treatment of Psoriasis: A Case Report of Long-Lasting Alopecia
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Successful induction of oral tolerance in Netherton syndrome
- Enhanced Insights into Frontal Fibrosing Alopecia: Advancements in Pathogenesis Understanding and Management Strategies
- Frontal Fibrosing Alopecia: An Update on Pathogenesis, Diagnosis, and Treatment
- Aging in hair follicle stem cells and niche microenvironment
- Why Do Not All Chemotherapy Patients Lose Their Hair? Answering an Intriguing Question
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Diffuse loss of hair with papules
- A reasonable Response to Diphensiprone in Pediatric Alopecia Patient: A Case Report
- Disorders of hair in children
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia